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CAS 153724-93-7

:

3-Chloropropenyl-1-boronic acid pinacol ester

Description:
3-Chloropropenyl-1-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a chloropropenyl moiety. This compound typically exhibits a pinacol ester structure, which enhances its stability and solubility in organic solvents. The presence of the chlorine atom introduces a degree of reactivity, making it useful in various synthetic applications, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The boronic acid functionality allows for the formation of carbon-boron bonds, which are pivotal in organic synthesis. Additionally, the pinacol ester form can facilitate the storage and handling of the boronic acid, as it is less prone to hydrolysis compared to its free acid counterpart. This compound is often utilized in the development of pharmaceuticals and agrochemicals, owing to its ability to participate in diverse chemical transformations. As with many organoboron compounds, it is essential to handle it with care, considering potential reactivity and toxicity associated with its components.
Formula:C9H16BClO2
Synonyms:
  • (E)-2-(3-Chloroprop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • trans-2-Chloromethylvinylboronic acid pinacol ester 97%
  • 2-[(1E)-3-chloroprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • (E)-3-Chloro-1-propene-1-boronic Acid Pinacol Ester
  • 3-Chloropropenyl-1-boronic acid pinacol ester
  • 2-[(E)-3-chloroprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 3-Chlorophenyl-1-boronic Acid Pinacol Ester
  • 2-[(E)-3-chloroprop-1-enyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-[(1E)-3-chloro-1-propen-1-yl]-4,4,5,5-tetramethyl-
  • 3-Chloropropenyl-1-boronic acid pinacol ester,2-(3-Chloro-propenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
  • (E)-2-(3-Chloro-1-propenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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